Lod ScorePedigreeGenetic LinkageChromosome MappingGenetic MarkersGenes, DominantMicrosatellite RepeatsChromosomes, Human, Pair 2Chromosomes, Human, Pair 1Genes, RecessiveHaplotypesConsanguinityGenotypeGenetic HeterogeneityQuantitative Trait LociModels, GeneticGenome, HumanPenetranceFamily HealthChromosomes, Human, Pair 6Nuclear FamilyChromosomes, Human, Pair 12Quantitative Trait, HeritableChromosomes, Human, Pair 16Chromosomes, Human, Pair 19PhenotypeGenetic Predisposition to DiseaseChromosomes, Human, Pair 7Chromosomes, Human, Pair 10Chromosomes, Human, Pair 5Chromosomes, Human, Pair 4Chromosomes, Human, Pair 3Chromosomes, Human, Pair 20AllelesChromosomes, Human, Pair 13X ChromosomeAge of OnsetChromosomes, Human, Pair 17SyndromeDNA Mutational AnalysisFamilyChromosomes, Human, Pair 9Genetic TestingUtahChromosomes, Human, Pair 11Likelihood FunctionsAdult ChildrenPolymorphism, Single NucleotideChromosomes, Human, Pair 15Linkage DisequilibriumSiblingsFounder EffectCataractChromosomes, HumanMutationHeterozygoteHomozygoteChromosomes, Human, Pair 8Inheritance PatternsChromosomes, Human, Pair 18Multifactorial InheritanceInbreedingPolymorphism, GeneticMatched-Pair AnalysisComputer SimulationGene FrequencyRecombination, GeneticGenetic Diseases, InbornRetinitis PigmentosaChromosomes, Human, Pair 14Polymorphism, Restriction Fragment LengthSoftwareHeterozygote DetectionGenetic VariationGenome-Wide Association StudyCrosses, GeneticBreedingMolecular Sequence DataChromosomes, Human, Pair 22Asian Continental Ancestry GroupAbnormalities, MultipleGenetic LociModels, StatisticalIcelandJewsBase SequenceChromosomes, MammalianChromosomes, Human, XMutation, MissenseReproducibility of ResultsPakistanEye Diseases, HereditaryNeoplastic Syndromes, HereditaryAlgorithmsHand Deformities, CongenitalHearing Loss, SensorineuralIntellectual DisabilityDNA, SatelliteMuscular DystrophiesFinland